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钯钴纳米颗粒在富氮碳纳米管中的共生作为析氢反应和氧还原反应的双功能电催化剂

Paragenesis of Palladium-Cobalt Nanoparticle in Nitrogen-Rich Carbon Nanotubes as a Bifunctional Electrocatalyst for Hydrogen-Evolution Reaction and Oxygen-Reduction Reaction.

作者信息

Huang Binbin, Chen Liyu, Wang Yan, Ouyang Liuzhang, Ye Jianshan

机构信息

College of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510641, P.R. China.

School of Materials Science and Engineering, Key Laboratory of Advanced Energy Storage Materials of Guangdong Province, South China University of Technology, Guangzhou, 510641, P.R. China.

出版信息

Chemistry. 2017 Jun 7;23(32):7710-7718. doi: 10.1002/chem.201700544. Epub 2017 Apr 6.

Abstract

The hydrogen evolution reaction (HER) and the oxygen reduction reaction (ORR) play important roles in many energy conversion and storage systems. To accelerate the reaction processes, there is a constant need for efficient new catalysts. In the present work, we have developed a facile pyrolysis-based process for the co-synthesis of palladium-cobalt nanoparticles supported on carbon nanotubes (Pd-CoCNTs), which exhibit superior catalytic activity for the HER and enhanced ORR performance. Non-agglomerated Pd nanoparticles of diameters 2-4 nm are uniformly distributed on the surface of CoCNTs, while the inner Co particles are an essential element in forming the framework of the CoCNTs. Compared to the Pd-free N-rich CoCNTs, Pd-CoCNTs have a more defective surface with a larger electrochemically active surface area (ECSA), and show enhanced ORR activity, outstanding methanol tolerance, and long-term stability in alkaline solution. At a low Pd loading of 0.0292 mg cm , the Pd-CoCNTs require overpotentials of 0.024 V and 0.215 V to catalyze the HER and to drive a current density of 50 mA cm in acidic solution, respectively. The palladium nanoparticles on the surface of the CoCNTs are considered to be highly active sites for HER, based on the results of control experiments, and it is easy to adjust the catalytic activity of the Pd-CoCNTs by changing the concentration of Pd therein. The proposed method provides a means of fabricating efficient bifunctional catalysts with controllable low contents of precious metals.

摘要

析氢反应(HER)和氧还原反应(ORR)在许多能量转换和存储系统中起着重要作用。为了加速反应过程,一直需要高效的新型催化剂。在本工作中,我们开发了一种基于热解的简便方法,用于共合成负载在碳纳米管上的钯-钴纳米颗粒(Pd-CoCNTs),其对析氢反应表现出优异的催化活性,并提高了氧还原反应性能。直径为2-4 nm的非团聚钯纳米颗粒均匀分布在CoCNTs表面,而内部的钴颗粒是形成CoCNTs框架的关键元素。与不含钯的富氮CoCNTs相比,Pd-CoCNTs具有更具缺陷的表面和更大的电化学活性表面积(ECSA),并在碱性溶液中表现出增强的氧还原反应活性、出色的甲醇耐受性和长期稳定性。在0.0292 mg cm的低钯负载量下,Pd-CoCNTs在酸性溶液中催化析氢反应和驱动50 mA cm电流密度分别需要0.024 V和0.215 V的过电位。基于对照实验结果,CoCNTs表面的钯纳米颗粒被认为是析氢反应的高活性位点,并且通过改变其中钯的浓度很容易调节Pd-CoCNTs的催化活性。所提出的方法提供了一种制备具有可控低贵金属含量的高效双功能催化剂的手段。

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